Flynn J N, Cannon C A, Sloan D, Neil J C, Jarrett O
Department of Veterinary Pathology, University of Glasgow, Bearsden, Glasgow, UK.
Immunology. 1999 Feb;96(2):220-9. doi: 10.1046/j.1365-2567.1999.00690.x.
Mitogen-activated lymphoblasts isolated from the blood and lymph nodes, but not the spleen, of domestic cats acutely infected with the Petaluma or Glasgow8 isolates of feline immunodeficiency virus (FIV), suppressed the replication of FIV in the MYA-1 T-cell line in a dose-dependent manner. This effect was not limited to the homologous isolate of FIV. The suppressor activity declined with progression to chronic infection, with lower levels of activity detectable only in the lymph nodes. Immunization of domestic cats with whole inactivated FIV vaccine elicited profound suppressor activity in both the blood and lymph nodes. The suppressor activity was associated with the CD8+ T-cell subpopulation, the effect did not appear to be major histocompatibility complex-restricted, and was mediated by a soluble factor(s). This activity may be associated with the control of virus replication during both the asymptomatic stages of FIV infection, and in the protective immunity observed in cats immunized with whole inactivated virus vaccines.
从急性感染了猫免疫缺陷病毒(FIV)派塔卢马株或格拉斯哥8株的家猫的血液和淋巴结而非脾脏中分离出的丝裂原活化淋巴细胞,以剂量依赖的方式抑制了FIV在MYA-1 T细胞系中的复制。这种效应并不局限于FIV的同源毒株。随着病情发展至慢性感染,抑制活性下降,仅在淋巴结中可检测到较低水平的活性。用全灭活FIV疫苗免疫家猫可在血液和淋巴结中引发显著的抑制活性。抑制活性与CD8 + T细胞亚群有关,这种效应似乎不受主要组织相容性复合体限制,且由一种或多种可溶性因子介导。这种活性可能与FIV感染无症状阶段的病毒复制控制以及用全灭活病毒疫苗免疫的猫所观察到的保护性免疫有关。